FUNG, Scott, Peter KWAN, Milotka FABRI, Andrzej HORBAN, Mijomir PELEMIS, Hie-Won HANN, Selim GUREL, Florin A. CARUNTU, John F. FLAHERTY, Benedetta MASSETTO, Kyungpil KIM, Kathryn M. KITRINOS, G. Mani SUBRAMANIAN, John G. MCHUTCHISON, Leland J. YEE, Magdy ELKHASHAB, Thomas BERG, Ioan SPOREA, Cihan YURDAYDIN, Petr HUSA, Maciej S. JABLKOWSKI a Edward GANE. Tenofovir disoproxil fumarate (TDF) vs. emtricitabine (FTC)/TDF in lamivudine resistant hepatitis B: A 5-year randomised study. Journal of Hepatology. Amsterdam: Elsevier Science BV, 2017, roč. 66, č. 1, s. 11-18. ISSN 0168-8278. Dostupné z: https://dx.doi.org/10.1016/j.jhep.2016.08.008.
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Základní údaje
Originální název Tenofovir disoproxil fumarate (TDF) vs. emtricitabine (FTC)/TDF in lamivudine resistant hepatitis B: A 5-year randomised study
Autoři FUNG, Scott (124 Kanada), Peter KWAN (124 Kanada), Milotka FABRI (688 Srbsko), Andrzej HORBAN (616 Polsko), Mijomir PELEMIS (688 Srbsko), Hie-Won HANN (840 Spojené státy), Selim GUREL (792 Turecko), Florin A. CARUNTU (642 Rumunsko), John F. FLAHERTY (840 Spojené státy), Benedetta MASSETTO (840 Spojené státy), Kyungpil KIM (840 Spojené státy), Kathryn M. KITRINOS (840 Spojené státy), G. Mani SUBRAMANIAN (840 Spojené státy), John G. MCHUTCHISON (840 Spojené státy), Leland J. YEE (840 Spojené státy), Magdy ELKHASHAB (124 Kanada), Thomas BERG (276 Německo), Ioan SPOREA (642 Rumunsko), Cihan YURDAYDIN (792 Turecko), Petr HUSA (203 Česká republika, garant, domácí), Maciej S. JABLKOWSKI (616 Polsko) a Edward GANE (554 Nový Zéland).
Vydání Journal of Hepatology, Amsterdam, Elsevier Science BV, 2017, 0168-8278.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30219 Gastroenterology and hepatology
Stát vydavatele Nizozemské království
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 15.040
Kód RIV RIV/00216224:14110/17:00095992
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1016/j.jhep.2016.08.008
UT WoS 000390642900003
Klíčová slova anglicky Bone mineral density; Emtricitabine; Lamivudine resistant; Renal function; Tenofovir disoproxil fumarate; Viral suppression
Štítky EL OK
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Soňa Böhmová, učo 232884. Změněno: 20. 3. 2018 15:44.
Anotace
Background & Aims: Long-term treatment with tenofovir disoproxil fumarate (TDF) alone, or in combination with emtricitabine (FTC) is associated with sustained viral suppression in patients with lamivudine resistant (LAM-R) chronic hepatitis B (CHB). Methods: LAM-R CHB patients were randomised 1:1 to receive TDF 300 mg or FTC 200 mg and TDF 300 mg once daily in a prospective, double blind, study. The proportion of patients with plasma hepatitis B virus (HBV) DNA <69 IU/m1 (<400 copies/ml) at week 96 (primary efficacy endpoint) was reported previously. Here we present week 240 follow-up data. Results: Overall, 280 patients were randomised to receive TDF (n = 141) or FTC/TDF (n = 139), and 85.4% completed 240 weeks of treatment. At week 240, 83.0% of patients in the TDF arm, and 82.7% of patients in the FTC/TDF treatment arm had HBV DNA <69 IU/ml (p = 0.96). Rates of normal alanine aminotransferase (ALT) and normalised ALT were similar between groups (p = 0.41 and p = 0.97 respectively). Hepatitis B e antigen loss and seroconversion at week 240 were similar between groups, (p = 0.41 and p = 0.67 respectively). Overall, six patients achieved hepatitis B surface antigen (HBsAg) loss and one patient (FTC/TDF arm) had HBsAg seroconversion by week 240. No TDF resistance was observed up to week 240. Treatment was generally well tolerated, and renal events were mild and infrequent (similar to 8.6%). The mean change in bone mineral density at week 240 was -0.98% and -2.54% at the spine and hip, respectively. Conclusions: TDF monotherapy was effective and well tolerated in LAM-R CHB patients for up to 240 weeks. Lay summary: The goal of oral antiviral treatment for chronic hepatitis B (CHB) is to achieve and maintain undetectable HBV DNA levels. Treatment options with enhanced potency, and low risk of resistance development for patients infected with lamivudine resistant (LAM-R) HBV are required. Tenofovir disoproxil fumarate (TDF) monotherapy was effective and well tolerated without TDF resistance development in CHB patients with LAM-R, for up to 240 weeks.
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